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27 results

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Defining new guidelines for screening the 22q11.2 deletion based on a clinical and dysmorphologic evaluation of 194 individuals and review of the literature.
Monteiro FP, Vieira TP, Sgardioli IC, Molck MC, Damiano AP, Souza J, Monlleó IL, Fontes MI, Fett-Conte AC, Félix TM, Leal GF, Ribeiro EM, Banzato CE, Dantas Cde R, Lopes-Cendes I, Gil-da-Silva-Lopes VL. Monteiro FP, et al. Among authors: leal gf. Eur J Pediatr. 2013 Jul;172(7):927-45. doi: 10.1007/s00431-013-1964-0. Epub 2013 Feb 26. Eur J Pediatr. 2013. PMID: 23440478
Three additional cases of the Michels syndrome.
Leal GF, Baptista EV. Leal GF, et al. Am J Med Genet A. 2007 Nov 15;143A(22):2747-50. doi: 10.1002/ajmg.a.32029. Am J Med Genet A. 2007. PMID: 17937425 No abstract available.
Poland anomaly with foot symbrachydactyly.
Silva EO, Leal GF, Carvalho VN. Silva EO, et al. Among authors: leal gf. Am J Med Genet. 2002 May 15;109(4):333-4. doi: 10.1002/ajmg.10377. Am J Med Genet. 2002. PMID: 11992491 No abstract available.
Implementing the brazilian database on orofacial clefts.
Monlleó IL, Fontes MÍ, Ribeiro EM, de Souza J, Leal GF, Félix TM, Fett-Conte AC, Bueno BH, Magna LA, Mossey PA, Gil-da Silva-Lopes V. Monlleó IL, et al. Among authors: leal gf. Plast Surg Int. 2013;2013:641570. doi: 10.1155/2013/641570. Epub 2013 Mar 12. Plast Surg Int. 2013. PMID: 23577250 Free PMC article.
27 results